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Nortriptyline hydrochloride Autophagy inhibitor

Cat.No.S3698

Nortriptyline hydrochloride (Desitriptyline, ELF-101, EN-7048, Desmethylamitriptyline) is the hydrochloride salt form of nortriptyline, a tricyclic antidepressant agent used for short-term treatment of various forms of depression.
Nortriptyline hydrochloride Autophagy inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 299.84

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Quality Control

Batch: S369801 DMSO]59 mg/mL]false]Water]59 mg/mL]false]Ethanol]59 mg/mL]false Purity: 99.97%
99.97

Solubility

In vitro
Batch:

DMSO : 59 mg/mL (196.77 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : 59 mg/mL

Ethanol : 59 mg/mL

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In vivo
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Chemical Information, Storage & Stability

Molecular Weight 299.84 Formula

C19H21N.HCl

Storage (From the date of receipt)
CAS No. 894-71-3 Download SDF Storage of Stock Solutions

Synonyms Desitriptyline HCl, ELF-101 hydrochloride, EN-7048 hydrochloride, Desmethylamitriptyline hydrochloride Smiles CNCCC=C1C2=CC=CC=C2CCC3=CC=CC=C31.Cl

Mechanism of Action

In vitro
Nortriptyline inhibits the vascular Kv channels in a concentration-dependent and state-independent manner independently of serotonin reuptake inhibition. It is a tricyclic antidepressant. At the cellular level, nortriptyline is inhibitory to many proteins and responses such as astroglial inwardly rectifying Kir4.1 channels, human neutrophil phagocytosis and oxidative burst, human cytochrome P-450 enzymes, opioid receptors, Ca2+-activated K+ channels, and priming of human neutrophils. Nortriptyline induces a significant [Ca2+]i rise and decreases viability in PC3 cells, MG63 human osteosarcoma, and renal tubular cells. Nortriptyline also exhibits anticancer activity in several different types of cells. For example,in human cutaneous melanoma cells,NTP has a half maximal inhibitory concentration(IC50) of 9 μM compared with 27 μM and 33 μM for clomipramine and amitriptyline, respectively. Nortriptyline induces cell cycle arrest and apoptosis in TCCSUP and MBT-2 cells.
In vivo
Nortriptyline inhibits tumor growth in mice inoculated with MBT-2 cells. Low concentrations of NTP (0.1-5 μM) confer neuroprotective effects, downregulate cytosolic phospholipase A2, and prevent mitochondrial depolarization with minimal toxicity in both astrocytes and mice. In contrast, higher concentrations of NTP (10-50 μM) have anti-tumor effects on human osteosarcoma and cutaneous melanoma cells.
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